Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11144688
rs11144688
PCSK5
9 75927370 intron variant G/A snv 9.2E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2010 2013
dbSNP: rs2284746
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2010 2013
dbSNP: rs3791679
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2008 2013
dbSNP: rs572169
rs572169
GHSR
0.882 0.160 3 172447937 synonymous variant C/T snv 0.31 0.24
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2010 2013
dbSNP: rs7466269
rs7466269
FUBP3
9 130588697 intron variant A/G snv 0.33
CUI: C0489786
Disease: Height
Height 		0.700 1.000 3 2008 2013
dbSNP: rs10748128
rs10748128 		12 69433878 intergenic variant G/T snv 0.42
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs1490384
rs1490384 		6 126530014 intron variant C/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs17511102
rs17511102
CDC42EP3 ; LOC105374465
2 37733470 intron variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs1950500
rs1950500 		14 24361644 upstream gene variant T/C snv 0.68
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2079795
rs2079795 		17 61419288 regulatory region variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2093210
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2280470
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs2856321
rs2856321
ETV6
12 11702839 intron variant G/A snv 0.52
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs310405
rs310405 		6 81090645 intergenic variant G/A snv 0.45
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs3764419
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs42235
rs42235
CDK6
7 92618762 intron variant C/T snv 0.32
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs526896
rs526896
LOC107986452
5 135021015 intergenic variant T/A;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs7689420
rs7689420
HHIP ; HHIP-AS1
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs806794
rs806794
H2AC7 ; H2BC7 ; H3C4
6 26200449 3 prime UTR variant A/G snv 0.36
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs9967417
rs9967417
DYM
18 49433130 intron variant G/C;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2010 2013
dbSNP: rs10058074
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs10231759
rs10231759 		7 150815084 regulatory region variant T/C snv 0.41
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs1029534
rs1029534
JAZF1
7 28149464 intron variant T/C;G snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs10475992
rs10475992
FBXW11
5 171908289 intron variant C/T snv 0.42
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013